# Efficacy and safety of epsilon-aminohexanoic acid and tranexamic acid during posterior interbody fusion surgery

**Authors:** Dilixiati Ainiwaer, Ayinuer Tuersun, Jiang Li, Xiaomei Li

PMC · DOI: 10.3389/fsurg.2025.1661609 · Frontiers in Surgery · 2025-11-10

## TL;DR

This study compares the effectiveness and safety of two hemostatic drugs, EACA and TXA, during spinal surgery and finds them equally effective.

## Contribution

The study provides evidence that EACA can be a viable alternative to TXA in posterior lumbar interbody fusion surgery.

## Key findings

- EACA and TXA showed similar hemostatic effects and safety outcomes in spinal surgery.
- There was no significant difference in blood loss, transfusion rates, or hospitalization time between the two groups.
- EACA had lower postoperative total protein and international normalized ratio compared to TXA.

## Abstract

Tranexamic acid (TXA) is a proven effective and favored antifibrinolytic hemostatic drug, while epsilon-aminocaproic acid (EACA) has only recently been applied in the field of orthopedics. Few studies compare the efficacy of these two drugs in spinal surgery. We evaluated the hemostatic performance and safety of aminocaproic acid, and explored whether aminocaproic acid can be used as a substitute for TXA during posterior lumbar interbody fusion (PLIF) surgery, providing theoretical support for the flexible selection of hemostatic drugs during spinal surgery.

We conducted retrospective analysis of 180 patients with lumbar disc herniation, lumbar spinal stenosis, and lumbar spondylolisthesis, who had been admitted to the spinal surgery department of the Our hospital or The Sixth Affiliated Hospital of Xinjiang Medical University, between September 2021 and May 2023, and underwent PLIF. According to the types of hemostatic drugs used during the perioperative period, the patients were divided into two groups, namely, the EACA group (n = 86) and the TXA group (n = 94). The main outcome measures were total blood loss, total red blood cell loss, and transfusion volume/rate. Other outcome measures included length of hospital stay, hospitalization costs, deep vein thrombosis rate, and biochemical hematological indicators, specifically indicators related to anemia, nutrition, and coagulation.

(1) The red blood cell width of the EACA group (43.94 ± 10.56) was significantly higher than that of the TXA group (40.45 ± 12.54), with a statistically significant difference (p < 0.05). (2) The postoperative total protein of the EACA group (56.17 ± 7.83) was significantly lower than that of the TXA group (59.3628 ± 6.73), with a statistically significant difference (p < 0.05). (3) The postoperative international normalized ratio of the EACA group (1.06 ± 0.14) was significantly lower than that of the TXA group (1.14 ± 0.13), with a statistically significant difference (p < 0.05). There was no statistically significant difference between the two groups in terms of other indicators.

There was no significant difference in total blood loss, total red blood cell loss, transfusion volume/rate, postoperative hospitalization time, hospitalization costs, and surgical complications between the intravenous EACA and TXA groups during PLIF surgery. The two groups had similar hemostatic effects and safety outcomes. Therefore, when selecting antifibrinolytic drugs during PLIF surgery, EACA can be considered an alternative to TXA. However, large-scale, multicenter randomized controlled studies are still required to gauge its later-stage efficacy.

## Linked entities

- **Chemicals:** epsilon-aminohexanoic acid (PubChem CID 564), tranexamic acid (PubChem CID 5526)
- **Diseases:** lumbar spinal stenosis (MONDO:0005965)

## Full-text entities

- **Diseases:** deep vein thrombosis (MESH:D020246), red blood cell loss (MESH:C562718), lumbar spondylolisthesis (MESH:D013168), coagulation (MESH:D001778), anemia (MESH:D000740), lumbar spinal stenosis (MESH:C563613), blood loss (MESH:D016063), lumbar disc herniation (MESH:C535531)
- **Chemicals:** TXA (MESH:D014148), EACA (MESH:D015119)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12620652/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12620652/full.md

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Source: https://tomesphere.com/paper/PMC12620652